ChatSpatial
Server Configuration
Describes the environment variables required to run the server.
| Name | Required | Description | Default |
|---|---|---|---|
No arguments | |||
Instructions
Guidance the server publishes about itself, which clients place ahead of the tool catalog so the model reads it before choosing anything.
This server publishes no instructions, or was last inspected before Glama recorded them.
Capabilities
Features and capabilities supported by this server
Protocol revision2025-11-25
| Capability | Details |
|---|---|
| tools | {
"listChanged": false
} |
| prompts | {
"listChanged": false
} |
| resources | {
"subscribe": false,
"listChanged": false
} |
| experimental | {} |
Tools
Functions exposed to the LLM to take actions
| Name | Description |
|---|---|
| load_dataA | Load spatial transcriptomics data with comprehensive metadata profile. |
| preprocess_dataA | Run QC, filtering, normalization, and highly variable gene selection. |
| compute_embeddingsB | Compute dimensionality reduction (PCA, UMAP), clustering, and neighbor graphs. |
| visualize_dataB | Visualize spatial transcriptomics data. Set plot_type and subtype in params; see VisualizationParameters schema for all options. |
| annotate_cell_typesB | Annotate cell types in spatial transcriptomics data. |
| analyze_spatial_statisticsC | Analyze spatial statistics and autocorrelation patterns. |
| find_markersC | Find differentially expressed genes between groups. |
| compare_conditionsA | Compare experimental conditions using pseudobulk differential expression (DESeq2). |
| analyze_cnvA | Analyze copy number variations (CNVs) in spatial transcriptomics data. |
| analyze_velocity_dataB | Analyze RNA velocity to understand cellular dynamics. Requires 'spliced' and 'unspliced' layers. |
| analyze_trajectory_dataC | Infer cellular trajectories and pseudotime ordering. |
| integrate_samplesB | Integrate multiple spatial transcriptomics samples into a unified dataset. |
| deconvolve_dataA | Deconvolve spatial spots to estimate cell type proportions. |
| identify_spatial_domainsC | Identify spatial domains and tissue architecture. |
| analyze_cell_communicationC | Analyze cell-cell communication and ligand-receptor interaction patterns. |
| analyze_enrichmentC | Perform gene set enrichment analysis. |
| find_spatial_genesC | Identify spatially variable genes. |
| register_spatial_dataC | Register/align spatial transcriptomics data across sections |
| export_dataA | Export dataset to disk for external script access. |
| reload_dataA | Reload dataset from disk after external script modifications. |
Prompts
Interactive templates invoked by user choice
| Name | Description |
|---|---|
No prompts | |
Resources
Contextual data attached and managed by the client
| Name | Description |
|---|---|
No resources | |
TDQS
Scored across 20 tools
Tools map to distinct analytical tasks such as loading, preprocessing, embedding, annotation, and downstream analyses, with descriptions that clarify each tool's role. However, 'find_markers' and 'compare_conditions' both involve differential expression and could be confused, and 'analyze_spatial_statistics' overlaps somewhat with 'find_spatial_genes'.
Nearly all tools follow a consistent verb_noun pattern like load_data, visualize_data, and analyze_enrichment. The naming is predictable and uniform, making tool selection straightforward.
20 tools is on the heavy side and sits in the 16-25 range that feels bloated for a typical MCP server. Each tool does appear to serve a distinct stage in the spatial transcriptomics workflow, but the overall surface is large.
The set covers the full analysis lifecycle from data loading, preprocessing, embedding, annotation, and a wide range of downstream analyses through export/reload. Minor gaps include no list/delete data management tools and no explicit metadata retrieval tool after loading, but these are workable.